Works matching IS 02719142 AND DT 2016 AND VI 36
Results: 123
Autoimmune and Inflammatory Manifestations in 247 Patients with Primary Immunodeficiency-a Report from the Slovenian National Registry.
- Published in:
- Journal of Clinical Immunology, 2016, v. 36, n. 8, p. 764, doi. 10.1007/s10875-016-0330-1
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- Publication type:
- Article
'How I manage' IgG4-Related Disease.
- Published in:
- Journal of Clinical Immunology, 2016, v. 36, n. 8, p. 754, doi. 10.1007/s10875-016-0331-0
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- Publication type:
- Article
CTP Synthase 1 Deficiency in Successfully Transplanted Siblings with Combined Immune Deficiency and Chronic Active EBV Infection.
- Published in:
- 2016
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- Publication type:
- Letter
Clinical, Immunological, and Molecular Findings of Patients with p47 Defect Chronic Granulomatous Disease (CGD) in Indian Families.
- Published in:
- Journal of Clinical Immunology, 2016, v. 36, n. 8, p. 774, doi. 10.1007/s10875-016-0333-y
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- Publication type:
- Article
Ataxia telangiectasia associated with nodular regenerative hyperplasia.
- Published in:
- 2016
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- Publication type:
- Letter
Asthma and Hypogammaglobulinemia: an Asthma Phenotype with Low Type 2 Inflammation.
- Published in:
- Journal of Clinical Immunology, 2016, v. 36, n. 8, p. 810, doi. 10.1007/s10875-016-0335-9
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- Publication type:
- Article
Neurologic Complications of Common Variable Immunodeficiency.
- Published in:
- Journal of Clinical Immunology, 2016, v. 36, n. 8, p. 793, doi. 10.1007/s10875-016-0336-8
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- Publication type:
- Article
Primary Immunodeficiency Diseases in Oman: 10-Year Experience in a Tertiary Care Hospital.
- Published in:
- Journal of Clinical Immunology, 2016, v. 36, n. 8, p. 785, doi. 10.1007/s10875-016-0337-7
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- Publication type:
- Article
Familial Chronic Granulomatous Disease Affecting Three Siblings and Causing Recurrent Tuberculosis.
- Published in:
- 2016
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- Publication type:
- Letter
A Novel Mutation in a Critical Region for the Methyl Donor Binding in DNMT3B Causes Immunodeficiency, Centromeric Instability, and Facial Anomalies Syndrome (ICF).
- Published in:
- Journal of Clinical Immunology, 2016, v. 36, n. 8, p. 801, doi. 10.1007/s10875-016-0340-z
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- Publication type:
- Article
The Importance of Measuring IL10 Levels in Patients with Suspected IL10/IL10R Defects.
- Published in:
- 2016
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- Publication type:
- Letter
Magnetic Resonance Imaging of Lungs as a Radiation-Free Technique for Lung Pathologies in Immunodeficient patients.
- Published in:
- 2016
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- Publication type:
- Letter
Patterns of Primary Immunodeficiency Disorders Among a Highly Consanguineous Population: Cairo University Pediatric Hospital's 5-Year Experience.
- Published in:
- Journal of Clinical Immunology, 2016, v. 36, n. 7, p. 649, doi. 10.1007/s10875-016-0314-1
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- Publication type:
- Article
Brain Abscess in a Child with Leukocyte Adhesion Defect: An Unusual Association.
- Published in:
- 2016
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- Publication type:
- Letter
Long-Term Outcomes of Hematopoietic Stem Cell Transplantation for ZAP70 Deficiency.
- Published in:
- Journal of Clinical Immunology, 2016, v. 36, n. 7, p. 713, doi. 10.1007/s10875-016-0316-z
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- Publication type:
- Article
Fatal Lymphoproliferative Disease in Two Siblings Lacking Functional FAAP24.
- Published in:
- Journal of Clinical Immunology, 2016, v. 36, n. 7, p. 684, doi. 10.1007/s10875-016-0317-y
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- Publication type:
- Article
Treatment of CGD-associated Colitis with the IL-23 Blocker Ustekinumab.
- Published in:
- 2016
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- Publication type:
- Letter
Thoracic Surgery in Chronic Granulomatous Disease: a 25-Year Single-Institution Experience.
- Published in:
- Journal of Clinical Immunology, 2016, v. 36, n. 7, p. 677, doi. 10.1007/s10875-016-0319-9
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- Publication type:
- Article
X-linked Inhibitor of Apoptosis Complicated by Granulomatous Lymphocytic Interstitial Lung Disease (GLILD) and Granulomatous Hepatitis.
- Published in:
- Journal of Clinical Immunology, 2016, v. 36, n. 7, p. 733, doi. 10.1007/s10875-016-0320-3
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- Publication type:
- Article
Phenotypic and Functional Comparison of Class Switch Recombination Deficiencies with a Subgroup of Common Variable Immunodeficiencies.
- Published in:
- Journal of Clinical Immunology, 2016, v. 36, n. 7, p. 656, doi. 10.1007/s10875-016-0321-2
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- Publication type:
- Article
Leukocyte Adhesion Deficiency Type 1 (LAD1) with Expressed but Nonfunctional CD11/CD18.
- Published in:
- 2016
- By:
- Publication type:
- Letter
Protein Kinase C δ: a Gatekeeper of Immune Homeostasis.
- Published in:
- Journal of Clinical Immunology, 2016, v. 36, n. 7, p. 631, doi. 10.1007/s10875-016-0323-0
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- Publication type:
- Article
Lymphoma Secondary to Congenital and Acquired Immunodeficiency Syndromes at a Turkish Pediatric Oncology Center.
- Published in:
- Journal of Clinical Immunology, 2016, v. 36, n. 7, p. 667, doi. 10.1007/s10875-016-0324-z
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- Publication type:
- Article
Exploring Autoimmunity in a Cohort of Children with Genetically Confirmed Aicardi-Goutières Syndrome.
- Published in:
- Journal of Clinical Immunology, 2016, v. 36, n. 7, p. 693, doi. 10.1007/s10875-016-0325-y
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- Publication type:
- Article
Unrelated Hematopoietic Cell Transplantation in a Patient with Combined Immunodeficiency with Granulomatous Disease and Autoimmunity Secondary to RAG Deficiency.
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- Journal of Clinical Immunology, 2016, v. 36, n. 7, p. 725, doi. 10.1007/s10875-016-0326-x
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- Publication type:
- Article
Efficacy, Safety, and Pharmacokinetics of a Novel Human Immune Globulin Subcutaneous, 20 % in Patients with Primary Immunodeficiency Diseases in North America.
- Published in:
- Journal of Clinical Immunology, 2016, v. 36, n. 7, p. 700, doi. 10.1007/s10875-016-0327-9
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- Publication type:
- Article
Severe Early-Onset Combined Immunodeficiency due to Heterozygous Gain-of-Function Mutations in STAT1.
- Published in:
- Journal of Clinical Immunology, 2016, v. 36, n. 7, p. 641, doi. 10.1007/s10875-016-0312-3
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- Publication type:
- Article
Long-Term Tolerability, Safety, and Efficacy of Recombinant Human Hyaluronidase-Facilitated Subcutaneous Infusion of Human Immunoglobulin for Primary Immunodeficiency.
- Published in:
- Journal of Clinical Immunology, 2016, v. 36, n. 6, p. 571, doi. 10.1007/s10875-016-0298-x
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- Publication type:
- Article
A Founder Effect of c.257 + 2T > C Mutation in NCF2 Gene Underlies Severe Chronic Granulomatous Disease in Eleven Patients.
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- Journal of Clinical Immunology, 2016, v. 36, n. 6, p. 547, doi. 10.1007/s10875-016-0299-9
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- Publication type:
- Article
Expanded CD4 Effector/Memory T Cell Subset in APECED Produces Predominantly Interferon Gamma.
- Published in:
- Journal of Clinical Immunology, 2016, v. 36, n. 6, p. 555, doi. 10.1007/s10875-016-0302-5
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- Publication type:
- Article
Flebogamma 5 % DIF Intravenous Immunoglobulin for Replacement Therapy in Children with Primary Immunodeficiency Diseases.
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- Journal of Clinical Immunology, 2016, v. 36, n. 6, p. 583, doi. 10.1007/s10875-016-0303-4
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- Publication type:
- Article
Activated PI3-kinase δ Syndrome: Long-term Follow-up after Cord Blood Transplantation.
- Published in:
- 2016
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- Publication type:
- Letter
NF-κB1 Haploinsufficiency Causing Immunodeficiency and EBV-Driven Lymphoproliferation.
- Published in:
- Journal of Clinical Immunology, 2016, v. 36, n. 6, p. 533, doi. 10.1007/s10875-016-0306-1
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- Publication type:
- Article
X-linked Hyper IgM Syndrome Presenting as Pulmonary Alveolar Proteinosis.
- Published in:
- Journal of Clinical Immunology, 2016, v. 36, n. 6, p. 564, doi. 10.1007/s10875-016-0307-0
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- Publication type:
- Article
Efficacy, Safety, and Pharmacokinetics of a New 10 % Liquid Intravenous Immunoglobulin Containing High Titer Neutralizing Antibody to RSV and Other Respiratory Viruses in Subjects with Primary Immunodeficiency Disease.
- Published in:
- Journal of Clinical Immunology, 2016, v. 36, n. 6, p. 590, doi. 10.1007/s10875-016-0308-z
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- Publication type:
- Article
A Novel Mutation in IKBKG/NEMO Leads to Ectodermal Dysplasia with Severe Immunodeficiency (EDA-ID).
- Published in:
- 2016
- By:
- Publication type:
- Letter
The Expanding Spectrum of NFkB1 Deficiency.
- Published in:
- 2016
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- Publication type:
- Editorial
Pharmacokinetics, Safety, and Tolerability of Subcutaneous Immune Globulin Injection (Human), 10 % Caprylate/Chromatography Purified (GAMUNEX®-C) in Pediatric Patients with Primary Immunodeficiency Disease.
- Published in:
- Journal of Clinical Immunology, 2016, v. 36, n. 6, p. 600, doi. 10.1007/s10875-016-0311-4
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- Publication type:
- Article
Role of Flow Cytometry in the Diagnosis of Chronic Granulomatous Disease: the Egyptian Experience.
- Published in:
- Journal of Clinical Immunology, 2016, v. 36, n. 6, p. 610, doi. 10.1007/s10875-016-0297-y
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- Publication type:
- Article
The Potential and Limits of Hematopoietic Stem Cell Transplantation for the Treatment of Autosomal Dominant Hyper-IgE Syndrome.
- Published in:
- Journal of Clinical Immunology, 2016, v. 36, n. 5, p. 511, doi. 10.1007/s10875-016-0278-1
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- Publication type:
- Article
Health-Related Quality of Life and Health Resource Utilization in Patients with Primary Immunodeficiency Disease Prior to and Following 12 Months of Immunoglobulin G Treatment.
- Published in:
- Journal of Clinical Immunology, 2016, v. 36, n. 5, p. 450, doi. 10.1007/s10875-016-0279-0
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- Publication type:
- Article
A Difficult and Rare Diagnosis of Autoimmune Enteropathy in a Patient Affected by Down Syndrome.
- Published in:
- 2016
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- Publication type:
- Letter
Dominant Splice Site Mutations in PIK3R1 Cause Hyper IgM Syndrome, Lymphadenopathy and Short Stature.
- Published in:
- Journal of Clinical Immunology, 2016, v. 36, n. 5, p. 462, doi. 10.1007/s10875-016-0281-6
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- Publication type:
- Article
Use of Thrombopoietin-Receptor Agonist in CVID-Associated Immune Thrombocytopenia.
- Published in:
- 2016
- By:
- Publication type:
- Letter
Erratum to: Chronic and Invasive Fungal Infections in a Family with CARD9 Deficiency.
- Published in:
- 2016
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- Publication type:
- Erratum
Respiratory Health and Related Quality of Life in Patients with Congenital Agammaglobulinemia in the Northern Region of the UK.
- Published in:
- Journal of Clinical Immunology, 2016, v. 36, n. 5, p. 472, doi. 10.1007/s10875-016-0284-3
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- Publication type:
- Article
Immunodeficiency in a Child with 22q11.2 Microduplication Syndrome.
- Published in:
- 2016
- By:
- Publication type:
- Letter
Erratum to: Spondyloenchondrodysplasia Due to Mutations in ACP5: A Comprehensive Survey.
- Published in:
- 2016
- By:
- Publication type:
- Erratum
Switching Patients to Home-Based Subcutaneous Immunoglobulin: an Economic Evaluation of an Interprofessional Drug Therapy Management Program.
- Published in:
- Journal of Clinical Immunology, 2016, v. 36, n. 5, p. 502, doi. 10.1007/s10875-016-0288-z
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- Publication type:
- Article
Successful Hematopoietic Stem Cell Transplantation in a Patient with LPS-Responsive Beige-Like Anchor ( LRBA) Gene Mutation.
- Published in:
- Journal of Clinical Immunology, 2016, v. 36, n. 5, p. 480, doi. 10.1007/s10875-016-0289-y
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- Publication type:
- Article